P27A (p.Pro27Ala) variant of TNFRSF9 (Q07011)
P27A (p.Pro27Ala) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
P27A (p.Pro27Ala) variant details
- p.Pro27Ala
- gnomAD rs1639876493
- Missense
- Variant Prioritization Score for Impact Estimate 0.0776
- REVEL 0.07
- CADD 0.07
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available